510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MHZClass III

Stimulator, Vestibular Acceleration, Therapeutic

Unknown
FDA source (opens on fda.gov)

MHZ is the FDA product code for Stimulator, Vestibular Acceleration, Therapeutic, a class III device type. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 2 recalls.

Classification record

Product code
MHZ
Device name
Stimulator, Vestibular Acceleration, Therapeutic
Device class
Class III
Review panel
Unknown
Submission type
Contact ODE
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
2

Clearances, product code MHZ

By decision year
1 clearance under product code MHZ with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MHZ by decision year
YearClearances
19841

Applicants with the most clearances

Product code MHZ
Applicants holding the most 510(k) clearances under product code MHZ
ApplicantClearances
Kontron Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MHZ.